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Journal Abstract Search

254 related items for PubMed ID: 32019385

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  • 3. Molecular Characterization of β- and α-Globin Gene Mutations in Individuals with Borderline Hb A2 Levels.
    Satthakarn S, Panyasai S, Pornprasert S.
    Hemoglobin; 2020 Sep; 44(5):349-353. PubMed ID: 33023363
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  • 4. Two novel α2 gene mutations causing altered amino acid sequences produce a mild (Hb Kinshasa, HBA2: c.428A > T) and severe (HBA2: c.342-345insCC) α-thalassemia phenotype.
    Saller E, Dutly F, Frischknecht H.
    Hemoglobin; 2015 Sep; 39(2):144-6. PubMed ID: 25786670
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  • 5. A Novel Mutation of the α2-Globin Gene Causing α+-Thalassemia: Hb Nanning (HBA2: c.369_370delinsGA).
    Chen B, Lin L, Yi S, Chen Q, Wei H, Li G, Zheng C, He S, Qiu X.
    Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547
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  • 6. Various α-Thalassemia Genotype Combinations of the Saudi-Type Polyadenylation Signal Mutation (αT-Saudiα) in the Population of Bahrain: An Update of Genotype-Phenotype Analyses.
    Al Moamen NJ, Thabet A, Mahdi F, Newton H, Salman E.
    Hemoglobin; 2018 May; 42(3):166-170. PubMed ID: 30864492
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  • 7. A Novel α2-Globin Gene Mutation: Hb Debao [α31(B12)Arg→Trp; HBA2: c.94A>T].
    Lin L, Chen B, Yi S, Chen Q, Wei H, Li G, Zheng C, Qiu XX, He S.
    Hemoglobin; 2017 Jan; 41(1):65-67. PubMed ID: 28367658
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  • 8. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM.
    Hemoglobin; 2016 Jan; 40(2):75-84. PubMed ID: 26635043
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  • 15. A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.
    Farashi S, Faramarzi Garous N, Zeinali F, Vakili S, Ashki M, Imanian H, Najmabadi H, Azarkeivan A, Tamaddoni A.
    Hemoglobin; 2015 Jan; 39(3):196-200. PubMed ID: 25976776
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  • 16. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
    Viprakasit V, Ekwattanakit S, Chalaow N, Riolueang S, Wijit S, Tanyut P, Chat-Uthai N, Tachavanich K.
    Acta Haematol; 2014 Jan; 131(2):88-94. PubMed ID: 24081251
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  • 17. α-Thalassemia syndromes in the United Arab Emirates.
    Baysal E.
    Hemoglobin; 2011 Jan; 35(5-6):574-80. PubMed ID: 22074123
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  • 19. CODON 30 (-GAG) (α2): hematological parameters in heterozygotes and also patients with Hb H disease.
    Yang Y, Li DZ.
    Hemoglobin; 2013 Jan; 37(6):599-603. PubMed ID: 23822871
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  • 20. Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective.
    Karakaş Z, Koç B, Temurhan S, Elgün T, Karaman S, Asker G, Gençay G, Timur Ç, Yıldırmak ZY, Celkan T, Devecioğlu Ö, Aydın F.
    Turk J Haematol; 2015 Dec; 32(4):344-50. PubMed ID: 26377141
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